Canonical Allele Identifier: CA1061120822
Gene: ARAP2 HGNC NCBI

Linked Data

gnomAD v3: 4-35981489-C-A
gnomAD v4: 4-35981489-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.35981489C>A , CM000666.2:g.35981489C>A GRCh38
NC_000004.11:g.35983111C>A , CM000666.1:g.35983111C>A GRCh37
NC_000004.10:g.35659506C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000503225.5:n.1607+3741G>T
XR_925192.1:n.1460G>T